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A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD
Genetic modifiers of risk and age at onset in GBA associated Parkinson's disease and Lewy body dementia
Genome-wide screen identifies rs646776 near sortilin as a regulator of progranulin levels in human plasma
Heritability and genetic variance of dementia with Lewy bodies
Exome sequencing reveals VCP mutations as a cause of familial ALS
